Canonical Allele Identifier: CA1415115424

Gene: IFT80 TRIM59-IFT80 C3orf80

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282608T= , CM000665.2:g.160282608T=	GRCh38
NC_000003.11:g.160000396T= , CM000665.1:g.160000396T=	GRCh37
NC_000003.10:g.161483090T=	NCBI36
NG_022932.1:g.121925A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1386A= (IFT80) MANE Select	ENSP00000312778.7:p.Glu462=
ENST00000326448.11:c.1386A= (IFT80)	ENSP00000312778.7:p.Glu462=
ENST00000483465.5:c.975A= (IFT80)	ENSP00000418196.1:p.Glu325=
ENST00000483754.1:c.1899A= (TRIM59-IFT80)	ENSP00000456272.1:p.Glu633=
ENST00000487943.5:n.2605A= (IFT80)
ENST00000496589.5:c.975A= (IFT80)	ENSP00000420646.1:p.Glu325=
NM_001190241.1:c.975A= (IFT80)	NP_001177170.1:p.Glu325=
NM_001190242.1:c.975A= (IFT80)	NP_001177171.1:p.Glu325=
NM_020800.2:c.1386A= (IFT80)	NP_065851.1:p.Glu462=
XR_924138.1:n.2900-7064T= (C3orf80)
NR_148401.1:n.2094A= (TRIM59-IFT80)
NR_148402.1:n.3630A= (TRIM59-IFT80)
NR_148403.1:n.3897A= (TRIM59-IFT80)
NM_020800.3:c.1386A= (IFT80) MANE Select	NP_065851.1:p.Glu462=
NM_001190241.2:c.975A= (IFT80)	NP_001177170.1:p.Glu325=
NM_001190242.2:c.975A= (IFT80)	NP_001177171.1:p.Glu325=